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Heart Rhythm|June 2, 2026
Clinical, histological, and molecular associations of early and late recurrence after thoracoscopic ablation for atrial fibrillationZhenyu Dong, Marc M Terpstra, Alexander Farouk da Silva da Freitas, et al.Leukemia|January 19, 2023
Chronic lymphocytic leukemia presence impairs antigen-specific CD8+ T-cell responses through epigenetic reprogramming towards short-lived effectorsAnne W J Martens, Inga Kavazović, Mia Krapić, et al.Acta Neuropathologica Communications|October 16, 2019
Profiling the unique protective properties of intracranial arterial endothelial cellsDorien M A Hermkens, Olga C G Stam, Nienke M de Wit, et al.Scientific Reports|March 2, 2022
Reduced ech-6 expression attenuates fat-induced lifespan shortening in C. elegansYasmine J Liu, Arwen W Gao, Reuben L Smith, et al.Mitochondrion|August 29, 2017
AMC-Bio-Artificial Liver culturing enhances mitochondrial biogenesis in human liver cell lines: The role of oxygen, medium perfusion and 3D configurationAziza A A Adam, Martien van Wenum, Vincent A van der Mark, et al.Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|August 16, 2018
HepaRG-Progenitor Cell Derived Hepatocytes Cultured in Bioartificial Livers Are Protected from Healthy- and Acute Liver Failure-Plasma Induced ToxicityMartien van Wenum, Philipp Treskes, Aziza A A Adam, et al.Neuromuscular Disorders : NMD|December 20, 2022
Pathogenic variants in three families with distal muscle involvementMarian A J Weterman, Marieke Bronk, Aldo Jongejan, et al.Cell and Tissue Research|October 13, 2023
MicroRNAs in atrial fibrillation target genes in structural remodellingNicoline W E van den Berg, Makiri Kawasaki, Fransisca A Nariswari, et al.Metabolism: Clinical and Experimental|June 13, 2021
Four-and-a-half LIM domain protein 2 (FHL2) deficiency protects mice from diet-induced obesity and high FHL2 expression marks human obesityMaria P Clemente-Olivo, Jayron J Habibe, Mariska Vos, et al.Human Molecular Genetics|October 10, 2014
CACNA1B mutation is linked to unique myoclonus-dystonia syndromeJustus L Groen, Arturo Andrade, Katja Ritz, et al.Pageof 13